A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987286



Internal ID12984168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:14109346..14123398hg38UCSC Ensembl
Innerchr5:14109455..14123507hg19UCSC Ensembl
Innerchr5:14162455..14176507hg18UCSC Ensembl
Innerchr5:14162455..14176507hg17UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg3814053
hg1914053
hg1814053
hg1714053
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752061
Supporting Variants
SamplesSPC_70
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987286
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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